Indications & Usage
Directions: FOR ORAL USE ONLY.
Scorodite Prunus Liquid
FDA Label NDC 48951-8168
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Uriel Pharmacy Inc. for the product Scorodite Prunus (NDC 48951-8168). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, warnings, otc - questions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Dosage & Administration
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
Otc - Active Ingredient
Active Ingredients: Camphora (Camphor) 4X, Veratrum (White hellebore) 4X, Prunus spinosa (Blackthorn) 6X, Scorodite (Nat. ferric arsenate) 6X, Hypophysis (Bovine pituitary gland) 8X, Aurum met. (Metallic gold) 10X
Inactive Ingredient
Inactive Ingredients: Water, Salt, Lactose
Otc - Purpose
Use: Temporary relief of headache.
Otc - Keep Out Of Reach Of Children
KEEP OUT OF REACH OF CHILDREN.
Warnings
Warnings: Do not use if allergic to any ingredient. Consult a doctor before use if lactose intolerant. Consult a doctor before use for serious conditions or if conditons worsen or persist. If pregnant or nursing consult a doctor before use. Natural ingredients may cause color, scent and/or taste variation.
Otc - Questions
Questions? Call 866.642.2858 Uriel, East Troy, WI 53120 www.urielpharmacy.com
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